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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504489Generated: October 30, 2026

N-Iodosuccinimide → 4-Bromo-5-fluoro-2-iodoaniline

https://huagongshe.com/reaction/1504489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant4-Bromo-3-fluoroanilineHCID 821848—
SolventAcetic AcidHCID 176—
SolventTolueneHCID 1140—
Product4-Bromo-5-fluoro-2-iodoanilineHCID 6865947687%

Reaction Steps

N-iodosuccinimide (2.90 ml, 28.9 mmol) was added to a solution of 4-bromo-3-fluoroaniline (5.00 g, 26.3 mmol) in AcOH (52.6 ml). The reaction was maintained at ambient temperature for 1.5 h, then diluted with 20 mL toluene and concentrated. The residue was dissolved in EtOAc and washed with 2 N aqueous NaOH. The organic phase was washed with brine, dried over sodium sulfate, filtered, and concentrated. The residue was purified by chromatography on silica gel (40-g Ultra SNAP column, 25-g silica gel loading column, 2-10% EtOAc/Heptane) to give 4-bromo-5-fluoro-2-iodoaniline (7.23 g, 22.89 mmol, 87% yield). 1H NMR (400 MHz, CHLOROFORM-d) δ 7.74-7.78 (m, 1H), 6.53-6.57 (m, 1H). m/z (ESI) 315.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212182B2
Source datasetuspto-grants-2015_12
ORD IDord-bfb13985fb9f4aa3b206201376e6d64b
Source noteuspto-grants-2015_12